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用于眼刺激试验的眼刺激试验验证研究。

Validation study on the Ocular Irritection assay for eye irritation testing.

作者信息

Eskes Chantra, Hoffmann Sebastian, Facchini Davide, Ulmer Rich, Wang Amy, Flego Manuela, Vassallo Marco, Bufo Monica, van Vliet Erwin, d'Abrosca Federica, Wilt Nathan

机构信息

SeCAM Services & Consultation on Alternative Methods, Agno, Switzerland.

seh consulting + services, Paderborn, Germany.

出版信息

Toxicol In Vitro. 2014 Aug;28(5):1046-65. doi: 10.1016/j.tiv.2014.02.009. Epub 2014 Mar 15.

DOI:10.1016/j.tiv.2014.02.009
PMID:24637247
Abstract

Both a prospective and a retrospective validation study were undertaken to assess the suitability of the Ocular Irritection assay to discriminate ocular hazards as defined by the OECD and UN Globally Harmonized System (UN GHS) for classification. The primary focus of the study was to evaluate the usefulness of the Ocular Irritection assay to reliably discriminate chemicals not requiring classification (UN GHS non-classified), from classified chemicals (UN GHS Categories 1 and 2). Furthermore a post-hoc evaluation was carried out to evaluate the usefulness of the assay to discriminate chemicals inducing serious eye damage (UN GHS Category 1) from other classes. The prospective validation study was conducted between 2009 and 2012 following internationally agreed principles. A set of 56 coded test chemicals for which quality and/or peer-reviewed in vivo data were available were used to obtain prospective data on the assay's reliability (reproducibility within and between laboratories) and relevance (predictive capacity). The assay showed good within-laboratory variability, transferability including to a naïve laboratory, and between-laboratory concordance of classifications (82% for the discrimination of non-classified from classified chemicals, and 83% for the discrimination of Category 1 from other classes). The obtained prospective data were then combined with existing data on the Ocular Irritection collected from various sources, totaling 88 chemicals with parallel in vivo and in vitro data to obtain a comprehensive assessment of the test method performances. The enlarged dataset comprised 43 non-classified, 25 Category 2 and 20 Category 1 chemicals according to the UN GHS classification. When used for the identification of UN GHS non-classified versus classified materials (based on the existing cut-off of 12.5) the Ocular Irritection assay showed an overall a sensitivity of 93% and a specificity of 58%. An evaluation on possible reasons for misclassification identified some organic functional groups (acrylate, carboxamide and cycloalkene) to correlate with the observed mispredictions. If these functional groups were excluded from the Ocular Irritection applicability domain, the obtained dataset (n=79 chemicals distributed as 41 UN GHS Classified and 38 Non-Classified chemicals) had an overall sensitivity of 98%, and specificity of 63%, which is in line with currently adopted test methods. When used for the identification of UN GHS Category 1 versus other categories (based on the existing cut-off of 30.0) the Ocular Irritection assay showed an overall specificity of 81% and a sensitivity of 50% which is again in line with currently adopted test methods. The Ocular Irritection assay appeared therefore as a useful test method to predict chemicals not requiring classification for eye hazards according to the UN GHS classification system. Furthermore the method was found suitable to identify serious/irreversible eye damage (UN GHS Category 1). The detailed documentation and results of the study have been submitted to an internationally recognized validation centre for peer-review.

摘要

开展了一项前瞻性验证研究和一项回顾性验证研究,以评估眼刺激试验对于区分经合组织(OECD)和联合国全球统一制度(UN GHS)所定义的眼部危害进行分类的适用性。该研究的主要重点是评估眼刺激试验对于可靠区分无需分类的化学品(UN GHS未分类)与已分类化学品(UN GHS第1类和第2类)的有用性。此外,还进行了事后评估,以评估该试验对于区分导致严重眼损伤的化学品(UN GHS第1类)与其他类别的有用性。前瞻性验证研究于2009年至2012年期间按照国际公认原则进行。使用一组56种编码测试化学品,这些化学品具有可获得的质量和/或同行评审的体内数据,以获取关于该试验可靠性(实验室内部和实验室之间的可重复性)和相关性(预测能力)的前瞻性数据。该试验显示出良好的实验室内部变异性、可转移性(包括转移到一个新实验室)以及实验室之间分类的一致性(区分未分类与已分类化学品的一致性为82%,区分第1类与其他类别的一致性为83%)。然后将获得的前瞻性数据与从各种来源收集的关于眼刺激的现有数据相结合,共有88种化学品具有平行的体内和体外数据,以全面评估测试方法的性能。根据UN GHS分类,扩大后的数据集包括43种未分类化学品、25种第2类化学品和20种第1类化学品。当用于识别UN GHS未分类与已分类物质时(基于现有的12.5的临界值),眼刺激试验总体灵敏度为93%,特异性为58%。对误分类的可能原因进行的评估确定了一些有机官能团(丙烯酸酯、羧酰胺和环烯烃)与观察到的错误预测相关。如果将这些官能团排除在眼刺激适用性范围之外,所获得的数据集(n = 79种化学品,分布为41种UN GHS已分类化学品和38种未分类化学品)总体灵敏度为98%,特异性为63%,这与目前采用的测试方法一致。当用于识别UN GHS第1类与其他类别时(基于现有的30.0临界值),眼刺激试验总体特异性为81%,灵敏度为50%,这也再次与目前采用的测试方法一致。因此,眼刺激试验似乎是一种有用的测试方法,可根据UN GHS分类系统预测无需进行眼部危害分类的化学品。此外,发现该方法适用于识别严重/不可逆眼损伤(UN GHS第1类)。该研究的详细文件和结果已提交给一个国际认可的验证中心进行同行评审。

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引用本文的文献

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